Syntaxin 1 Polyclonal Antibody

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商品货号： PLA019106

适应性： 人,小鼠,大鼠

￥600元

规格：

40μL 100μL 200μL

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MSDS

说明书

商品描述

基因名称： STX1A
蛋白名称： Syntaxin-1A
Human_gene_id： 6804
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=6804
Human_swiss_prot_no： Q16623
Human_swiss_link： http://www.uniprot.org/uniprotkb/Q16623/entry
Mouse_gene_id： 20907
Mouse_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=20907
Mouse_swiss_prot_no： O35526
Mouse_swiss_link： http://www.uniprot.org/uniprot/O35526
Rat_gene_id： 116470
Rat_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=116470
Rat_swiss_prot_no： P32851
Rat_swiss_link： http://www.uniprot.org/uniprot/P32851
特异性： Syntaxin 1 Polyclonal Antibody detects endogenous levels of Syntaxin 1 protein.
组成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
来源： Polyclonal, Rabbit,IgG
稀释： WB 1:500 - 1:2000. IHC-p: 1:100-1:300. ELISA: 1:20000.. IF 1:50-200
纯化工艺： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
浓度： 1 mg/ml
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
说明书： 1
Msds： MSDS_Antibody.pdf
其他名称： STX1A; STX1; Syntaxin-1A; Neuron-specific antigen HPC-1
实测条带： 30kD
信号通路： SNARE interactions in vesicular transport;
功能： disease:Haploinsufficiency of STX1A may be the cause of certain cardiovascular and musculo-skeletal abnormalities observed in Williams-Beuren syndrome (WBS), a rare developmental disorder. It is a contiguous gene deletion syndrome involving genes from chromosome band 7q11.23.,function:Potentially involved in docking of synaptic vesicles at presynaptic active zones. May play a critical role in neurotransmitter exocytosis.,similarity:Belongs to the syntaxin family.,similarity:Contains 1 t-SNARE coiled-coil homology domain.,subunit:Part of the SNARE core complex containing SNAP25, VAMP2 and STX1A. This complex binds to CPLX1. Binds SYTL4 and STXBP6. Found in a ternary complex with STX1A and SNAP25. Interacts with OTOF (By similarity). Found in a complex with VAMP8 and SNAP23. Interacts with VAPA and SYBU.,tissue specificity:Isoform 1 is highly expressed in embryonic spinal chord and ganglia and in adult cerebellum and cerebral cortex. Isoform 2 is expressed in heart, liver, fat, skeletal muscle, kidney and brain.,
相关产品： YT5440,YT4493,YP0569,RS0001,RS0002,YM3028,YM3029
细胞定位： Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane ; Single-pass type IV membrane protein . Cell junction, synapse, synaptosome . Cell membrane . Colocalizes with KCNB1 at the cell membrane. .; [Isoform 2]: Secreted .
组织表达： [Isoform 1]: Highly expressed in embryonic spinal cord and ganglia and in adult cerebellum and cerebral cortex. ; [Isoform 2]: Expressed in heart, liver, fat, skeletal muscle, kidney and brain.
科研货号： PLA019106

Syntaxin 1 Polyclonal Antibody

Catalog No PLA019106

Product information

基因名称： STX1A
蛋白名称： Syntaxin-1A
Human_gene_id： 6804
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=6804
Human_swiss_prot_no： Q16623
Human_swiss_link： http://www.uniprot.org/uniprotkb/Q16623/entry
Mouse_gene_id： 20907
Mouse_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=20907
Mouse_swiss_prot_no： O35526
Mouse_swiss_link： http://www.uniprot.org/uniprot/O35526
Rat_gene_id： 116470
Rat_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=116470
Rat_swiss_prot_no： P32851
Rat_swiss_link： http://www.uniprot.org/uniprot/P32851
特异性： Syntaxin 1 Polyclonal Antibody detects endogenous levels of Syntaxin 1 protein.
组成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
来源： Polyclonal, Rabbit,IgG
稀释： WB 1:500 - 1:2000. IHC-p: 1:100-1:300. ELISA: 1:20000.. IF 1:50-200
纯化工艺： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
浓度： 1 mg/ml
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
说明书： 1
Msds： MSDS_Antibody.pdf
其他名称： STX1A; STX1; Syntaxin-1A; Neuron-specific antigen HPC-1
实测条带： 30kD
信号通路： SNARE interactions in vesicular transport;
功能： disease:Haploinsufficiency of STX1A may be the cause of certain cardiovascular and musculo-skeletal abnormalities observed in Williams-Beuren syndrome (WBS), a rare developmental disorder. It is a contiguous gene deletion syndrome involving genes from chromosome band 7q11.23.,function:Potentially involved in docking of synaptic vesicles at presynaptic active zones. May play a critical role in neurotransmitter exocytosis.,similarity:Belongs to the syntaxin family.,similarity:Contains 1 t-SNARE coiled-coil homology domain.,subunit:Part of the SNARE core complex containing SNAP25, VAMP2 and STX1A. This complex binds to CPLX1. Binds SYTL4 and STXBP6. Found in a ternary complex with STX1A and SNAP25. Interacts with OTOF (By similarity). Found in a complex with VAMP8 and SNAP23. Interacts with VAPA and SYBU.,tissue specificity:Isoform 1 is highly expressed in embryonic spinal chord and ganglia and in adult cerebellum and cerebral cortex. Isoform 2 is expressed in heart, liver, fat, skeletal muscle, kidney and brain.,
相关产品： YT5440,YT4493,YP0569,RS0001,RS0002,YM3028,YM3029
细胞定位： Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane ; Single-pass type IV membrane protein . Cell junction, synapse, synaptosome . Cell membrane . Colocalizes with KCNB1 at the cell membrane. .; [Isoform 2]: Secreted .
组织表达： [Isoform 1]: Highly expressed in embryonic spinal cord and ganglia and in adult cerebellum and cerebral cortex. ; [Isoform 2]: Expressed in heart, liver, fat, skeletal muscle, kidney and brain.
科研货号： PLA019106

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